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番茄红素通过调节 SIRT3 介导的通路减轻邻苯二甲酸二(2-乙基己基)酯诱导的脾线粒体自噬。

Lycopene attenuates di(2-ethylhexyl) phthalate-induced mitophagy in spleen by regulating the sirtuin3-mediated pathway.

机构信息

College of Veterinary Medicine, Northeast Agricultural University, Harbin, 150030, P. R. China.

出版信息

Food Funct. 2021 May 21;12(10):4582-4590. doi: 10.1039/d0fo03277h. Epub 2021 Apr 28.

Abstract

Lycopene (Lyc) has been discussed as a potential effector in the prevention and therapy of various diseases. Di(2-ethylhexyl) phthalate (DEHP) is regarded as a universal environmental pollutant. To clarify the potential protective effect of Lyc on DEHP-induced splenic injury, 140 male mice were randomized into seven groups: control (distilled water), vehicle control (corn oil per day), Lyc (5 mg per kg BW per day), DEHP (500 or 1000 mg per kg BW per day), and DEHP combined Lyc group, respectively. All experimental animals were treated by oral gavage for 28 days. The results that showed DEHP exposure significantly up-regulated the mRNA and protein expression of the sirtuin family (except SIRT4-5), PGC-1α, OPA1, Drp1, MFN1/2, NRF1, TFAM, Parkin and PINK in DEHP-treated alone groups and the SOD2 and LC3-II protein expression were also in accordance with the above changes. These were accompanied with an increase of the number of inflammatory cells and rate of mitochondrial damage, and autophagosome formation in the spleen. Notably, Lyc supplementation facilitated all these changes to effectively return to the normal level, indicating that Lyc exerts protective effects against DEHP-induced splenic toxicity. Altogether, the protective effects of Lyc may be a strategy to ameliorate DEHP-induced spleen damage.

摘要

番茄红素(Lyc)被认为是一种潜在的效应物,可预防和治疗多种疾病。邻苯二甲酸二(2-乙基己基)酯(DEHP)被认为是一种普遍存在的环境污染物。为了阐明 Lyc 对 DEHP 诱导的脾脏损伤的潜在保护作用,将 140 只雄性小鼠随机分为七组:对照组(蒸馏水)、玉米油对照组(每天 1 次)、Lyc 组(5mg/kgBW/天)、DEHP 组(500 或 1000mg/kgBW/天)和 DEHP 联合 Lyc 组,分别。所有实验动物均通过口服灌胃处理 28 天。结果表明,DEHP 暴露显著上调了 Sirtuin 家族(除 SIRT4-5 外)、PGC-1α、OPA1、Drp1、MFN1/2、NRF1、TFAM、Parkin 和 PINK 的 mRNA 和蛋白表达,同时 SOD2 和 LC3-II 蛋白表达也与上述变化一致。这些变化伴随着脾脏中炎症细胞数量的增加和线粒体损伤以及自噬体形成的增加。值得注意的是,Lyc 的补充促进了所有这些变化有效地恢复到正常水平,表明 Lyc 对 DEHP 诱导的脾脏毒性具有保护作用。总之,Lyc 的保护作用可能是一种改善 DEHP 诱导的脾脏损伤的策略。

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